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Acta Neurochirurgica
|
October 14, 2020
Globus pallidus internus activity during simultaneous bilateral microelectrode recordings in status dystonicus
Vincenzo Levi, A Franzini, S Rinaldo, et al.
Neurology
|
January 29, 2003
Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency
N Nardocci, G Zorzi, N Blau, et al.
Journal of Inherited Metabolic Disease
|
August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutations
B Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Neurology
|
May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria
N Nardocci, G Zorzi, L Farina, et al.
Neuropediatrics
|
August 31, 2011
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration
L Chiapparini, M Savoiardo, S D'Arrigo, et al.
Neurogenetics
|
July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome
A Catania, R Battini, T Pippucci, et al.
European Journal of Neurology
|
March 23, 2016
Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration
I Kraoua, M Romani, D Tonduti, et al.
Brain & Development
|
October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum
A Iodice, M Carecchio, G Zorzi, et al.
Brain & Development
|
May 5, 2019
Corrigendum to "Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum" [Brain Dev. 41 (2019) 250-256]
A Iodice, M Carecchio, G Zorzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families
C Mariotti, C Gellera, M Rimoldi, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
Acta Neurochirurgica
|
October 14, 2020
Globus pallidus internus activity during simultaneous bilateral microelectrode recordings in status dystonicus
Vincenzo Levi, A Franzini, S Rinaldo, et al.
Neurology
|
January 29, 2003
Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency
N Nardocci, G Zorzi, N Blau, et al.
Journal of Inherited Metabolic Disease
|
August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutations
B Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Neurology
|
May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria
N Nardocci, G Zorzi, L Farina, et al.
Neuropediatrics
|
August 31, 2011
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration
L Chiapparini, M Savoiardo, S D'Arrigo, et al.
Neurogenetics
|
July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome
A Catania, R Battini, T Pippucci, et al.
European Journal of Neurology
|
March 23, 2016
Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration
I Kraoua, M Romani, D Tonduti, et al.
Brain & Development
|
October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum
A Iodice, M Carecchio, G Zorzi, et al.
Brain & Development
|
May 5, 2019
Corrigendum to "Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum" [Brain Dev. 41 (2019) 250-256]
A Iodice, M Carecchio, G Zorzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families
C Mariotti, C Gellera, M Rimoldi, et al.
Page
of 6